Unclassified - Pleasanton, CA

posted 5 months ago

Full-time - Senior
Remote - Pleasanton, CA
101-250 employees

About the position

The Senior SAS Programmer position at Maxis Clinical Sciences is a critical role that involves designing, developing, evaluating, and modifying SAS programs to analyze and evaluate clinical data. The successful candidate will work under moderate guidance and will be responsible for planning, writing, and executing statistical programs aimed at analyzing data from various databases. This includes producing tables, listings, and figures while ensuring data accuracy and consistency throughout the process. The role requires extensive knowledge and skills in programming, and the candidate may act as the lead programmer on project teams, consulting on the design and development of clinical trials, protocols, and case report forms. In addition to programming responsibilities, the Senior SAS Programmer will validate, document, and archive single-use programs, as well as maintain and validate the SAS macro library. The position also involves exploring new programming technologies, testing, documenting, and integrating software tools into programming procedures, and reviewing work processes and standard operating procedures (SOPs). The programmer will act as the SAS representative, coordinating licensing with other RMD sites, tracking the necessity of SAS patches, and validating SAS installations and updates. The role requires troubleshooting and resolving complex problems creatively, taking a fresh perspective on existing solutions, and implementing new concepts and methodologies. The Senior SAS Programmer will also lead internal and external teams, building professional relationships to ensure successful project outcomes. This position is remote, allowing for flexibility while contributing to a global team that operates 24/7 across North America, Europe, and Asia.

Responsibilities

  • Design, develop, evaluate, and modify SAS programs to analyze clinical data.
  • Plan, write, and execute statistical programs to analyze data from databases.
  • Produce tables, listings, and figures while assessing data accuracy and consistency.
  • Act as lead programmer on project teams and consult on clinical trial design and development.
  • Validate, document, and archive single-use programs and maintain the SAS macro library.
  • Explore new programming technologies and integrate software tools into programming procedures.
  • Document and review work processes and standard operating procedures (SOPs).
  • Act as SAS representative and coordinate licensing with other RMD sites.
  • Track necessity of SAS patches and validate SAS installations and updates.
  • Troubleshoot and resolve complex problems creatively and implement new methodologies.
  • Lead internal and external teams and build professional relationships.

Requirements

  • 10+ years of relevant work experience as a statistical programmer using SAS in a pharmaceutical, biotechnology, diagnostics, or medical device environment.
  • 10+ years of experience with MS or 2 years with PhD of relevant work experience as a statistical programmer using SAS.
  • Bachelor's degree in statistics, biostatistics, mathematics, computer science, or a related field, or equivalent combination of education.

Nice-to-haves

  • Experience with R programming and SAS Macros.
  • Familiarity with Python and VB skills.
© 2024 Teal Labs, Inc
Privacy PolicyTerms of Service